5-(7-Hydroxy-2-oxo-2H-chromene-3-carboxamido)pentanoic acid
95%
- Product Code: 87562
CAS:
1267539-46-7
| Molecular Weight: | 305.28 g./mol | Molecular Formula: | C₁₅H₁₅NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30185150 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development. Its structure, featuring a coumarin derivative, makes it a valuable scaffold for designing bioactive molecules. It is often explored for its potential as an anti-inflammatory, antioxidant, or antimicrobial agent. Researchers investigate its ability to interact with biological targets, such as enzymes or receptors, due to its unique combination of functional groups. Additionally, its fluorescent properties, derived from the coumarin moiety, make it useful in biochemical assays and imaging studies for tracking cellular processes. It is also studied for its role in synthesizing more complex molecules with therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿22,815.00 |
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5-(7-Hydroxy-2-oxo-2H-chromene-3-carboxamido)pentanoic acid
This compound is primarily utilized in the field of medicinal chemistry and drug development. Its structure, featuring a coumarin derivative, makes it a valuable scaffold for designing bioactive molecules. It is often explored for its potential as an anti-inflammatory, antioxidant, or antimicrobial agent. Researchers investigate its ability to interact with biological targets, such as enzymes or receptors, due to its unique combination of functional groups. Additionally, its fluorescent properties, derived from the coumarin moiety, make it useful in biochemical assays and imaging studies for tracking cellular processes. It is also studied for its role in synthesizing more complex molecules with therapeutic applications.
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